VANICREAM SUNSCREEN SPORT BROAD SPECTRUM SPF 35- zinc oxide cream 
Pharmaceutical Specialties, Inc.

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VANICREAM Sunscreen Sport Broad Spectrum SPF35

Drug Facts

Active ingredient

Zinc oxide 12%

Purpose

Sunscreen

Uses

Warnings

For external use only

Do not use on damaged or broken skin

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if rash occurs

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

protect this product from excessive heat and direct sun

Inactive ingredients allantoin, butyloctyl salicylate, C12-15 alkyl benzoate, caprylyl glycol, glyceryl behenate, glyceryl dibehenate, glyceryl stearate, lecithin, neopentyl glycol diheptanoate, 1,2-hexanediol, polyester-7, polyglyceryl-3 polyricinoleate, propanediol, silica, sodium chloride, squalane, tribehenin, tridecyl salicylate, water

Questions or Comments?

1-800-325-8232

www.vanicream.com

Vanicream is a trademark, or registered trademark, of Pharmaceutical Specialties, Inc. in the U.S. or other countries.

Dist. by

PHARMACEUTICAL SPECIALTIES, INC.

ROCHESTER, MN 55901 Made in U.S.A.

NDC 45334-331-03

DERMATOLOGIST TESTED

New Formula

VANICREAM™Sunscreen Sport

BROAD SPECTRUM SPF 35

MINERAL SUNSCREEN

WATER RESISTANT (80 MINUTES)

NON-COMEDOGENIC

Free of dyes, fragrance, masking fragrance, lanolin, parabens & formaldehyde releasers

Gluten-free

for Sensitive Skin

Net Wt 3 oz (85 g)

LABEL

VANICREAM SUNSCREEN SPORT BROAD SPECTRUM SPF 35 
zinc oxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:45334-331
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION12 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
GLYCERYL 1,3-DIBEHENATE (UNII: 84T2X52XS0)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
POLYESTER-7 (UNII: 0841698D2F)  
SQUALANE (UNII: GW89575KF9)  
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)  
PROPANEDIOL (UNII: 5965N8W85T)  
TRIDECYL SALICYLATE (UNII: AZQ08K38Z1)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
TRIBEHENIN (UNII: 8OC9U7TQZ0)  
WATER (UNII: 059QF0KO0R)  
POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
ALLANTOIN (UNII: 344S277G0Z)  
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
GLYCERYL MONOBEHENATE (UNII: A626UU0W2A)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:45334-331-031 in 1 CARTON04/27/202111/30/2024
185 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02004/27/202111/30/2024
Labeler - Pharmaceutical Specialties, Inc. (076499557)

Revised: 11/2023
Document Id: 09ab033c-2737-c85b-e063-6294a90a00cb
Set id: b5589aa0-2b1b-358e-e053-2995a90a549a
Version: 5
Effective Time: 20231108
 
Pharmaceutical Specialties, Inc.